Compatibility between aluminium nitride and nickel

Citation
T. Shimoo et al., Compatibility between aluminium nitride and nickel, J CERAM S J, 107(1), 1999, pp. 78-83
Citations number
35
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
JOURNAL OF THE CERAMIC SOCIETY OF JAPAN
ISSN journal
09145400 → ACNP
Volume
107
Issue
1
Year of publication
1999
Pages
78 - 83
Database
ISI
SICI code
0914-5400(199901)107:1<78:CBANAN>2.0.ZU;2-9
Abstract
In relation to the joining of aluminium nitride ceramics to metal, the reac tion products and the reaction mechanism between AIN and Ni have been inves tigated under a nitrogen or an argon atmosphere at temperatures of 1273-167 3 K. Using AIN-Ni powder mixtures, reaction rates were determined by thermo gravimetric analysis and the reaction products were examined by X-ray diffr action, The reaction between AIN and Ni occurred above 1250 K under both N- 2 and Ar atmosphere, Under Nz atmosphere, the reaction product was only a N i-Al solid solution, Under Ar atmosphere, at higher temperatures and on pro longed heating, the reaction product was changed in the following order: Ni -Al solid solution, Ni-Al(s.s.) + Ni3Al, Ni3Al, Ni3Al + NiAl and finally Ni Al. The initial rates of the reaction obeyed a linear rate law. Under both N-2 and Ar atmosphere, the rate constants and the activation energies (224 and 210 kJ/mol) showed comparable values, The reaction rate is thought to b e controlled by a chemical process, such as the dissociation of AIN, When t he Ni particles were covered with a reaciton layer, the rate obeyed a parab olic rate law, The rate constant under N-2 atmosphere was 2 orders of magni tude lower than that under Ar atmosphere, In the range of stability of Ni-A l(s.s.), the activation energy under N-2 atmosphere (124 kJ/mol) was almost identical to that under Ar atmosphere (127 kJ/mol). Under Ar atmosphere, t he activation energy for Ni3Al formation was 342 kJ/mol. The kinetics are p robably determined by solid-state diffusion through the reaction layer.